chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184595804045958041TG30GENIChomozygous119491447
184598535045985351TC40GENIChomozygous110331255
184599916545999166CT13GENIChomozygous110331257
184600001746000018CT31GENIChomozygous110331259
184600845046008451GA83GENICheterozygous119491448
184603586246035863GC16GENIChomozygous110331261
184605417146054172GT36GENICheterozygous119491449
184605418046054181CT37GENICheterozygous119491450
184605418446054185CT36GENICheterozygous119491451
184605927746059278TC29GENIChomozygous110331263
184606439346064394GA30GENICpossibly homozygous110331265
184609298646092987CT243GENICheterozygous119491452
184609324246093243GC73GENICheterozygous119491453
184610385646103857TC6GENIChomozygous110533576
184610467646104677TG110GENICheterozygous119491454
184610468646104687GT102GENICheterozygous119491455
184612553346125534CT28GENIChomozygous110331267
184613381846133819GA28GENIChomozygous110331269
184614961746149618CT47GENIChomozygous110331271